ICON plc is seeking a Clinical Research Associate II to contribute to trial monitoring activities in a agile workplace. You will conduct site visits, ensure protocol compliance, and maintain data integrity across Phase I studies, collaborating with investigators and site staff to drive study quality.
The role requires a Bachelor's degree in a scientific or healthcare-related field, at least 2 years of CRA experience, and the ability to travel up to 60% as needed.ICON offers a comprehensive
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📌 Phase I Cra Ii — Monitoring For High Impact Trials Manitoba
🏢 ICON Strategic Solutions
📍 Manitoba
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